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For: Schmid I, Klenk AK, Sparber-Sauer M, Koscielniak E, Maxwell R, Häberle B. Kaposiform hemangioendothelioma in children: a benign vascular tumor with multiple treatment options. World J Pediatr 2018;14:322-9. [PMID: 30054848 DOI: 10.1007/s12519-018-0171-5] [Cited by in Crossref: 21] [Cited by in F6Publishing: 11] [Article Influence: 5.3] [Reference Citation Analysis]
Number Citing Articles
1 Sparber-Sauer M, Koscielniak E, Vokuhl C, Schmid I, Bien E, Seitz G, Hallmen E, von Kalle T, Scheer M, Münter M, Bielack SS, Niggli F, Ljungman G, Fuchs J, Hettmer S, Rössler J, Klingebiel T; CWS Study Group. Endothelial cell malignancies in infants, children and adolescents: Treatment results of three Cooperative Weichteilsarkom Studiengruppe (CWS) trials and one registry. Pediatr Blood Cancer 2020;67:e28095. [PMID: 31814291 DOI: 10.1002/pbc.28095] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
2 Yao W, Li K, Wang Z, Wang J, Ji Y, Zhou L, Huang H, Gao X, Huang Z, Gu S, Yang H, Zheng S. Comparison of efficacy and safety of corticosteroid and vincristine in treating kaposiform hemangioendothelioma and tufted angioma: A multicenter prospective randomized controlled clinical trial. J Dermatol 2021;48:576-84. [PMID: 33608936 DOI: 10.1111/1346-8138.15767] [Reference Citation Analysis]
3 Ten Broek RW, Koelsche C, Eijkelenboom A, Mentzel T, Creytens D, Vokuhl C, van Gorp JM, Versleijen-Jonkers YM, van der Vleuten CJ, Kemmeren P, van de Geer E, von Deimling A, Flucke U. Kaposiform hemangioendothelioma and tufted angioma - (epi)genetic analysis including genome-wide methylation profiling. Ann Diagn Pathol 2020;44:151434. [PMID: 31887709 DOI: 10.1016/j.anndiagpath.2019.151434] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
4 Cataldo AM, de Jong MA, Gross M. Kaposiform Hemangioendothelioma of the middle ear in a pediatric patient: Outcomes following dual therapy with Sirolimus and Vincristine. International Journal of Pediatric Otorhinolaryngology Case Reports 2020;28-30:100681. [DOI: 10.1016/j.pedeo.2020.100681] [Reference Citation Analysis]
5 Massara B, Mariem R, Emna B, Meriam T, Faiza S, Sonia B, Meriem A, Lamia G, Tahia S, Hamida T. Kaposiform hemangioendothelioma with fatal income: Kasabach–Merritt phenomenon and hypercalcemia. Clinical Case Reports 2022;10. [DOI: 10.1002/ccr3.5458] [Reference Citation Analysis]
6 Brill R, Uller W, Huf V, Müller-Wille R, Schmid I, Pohl A, Häberle B, Perkowski S, Funke K, Till AM, Lauten M, Neumann J, Güttel C, Heid E, Ziermann F, Schmid A, Hüsemann D, Meyer L, Sporns PB, Schinner R, Schmidt VF, Ricke J, Rössler J, Kapp FG, Wohlgemuth WA, Wildgruber M. Additive value of transarterial embolization to systemic sirolimus treatment in kaposiform hemangioendothelioma. Int J Cancer 2021;148:2345-51. [PMID: 33231291 DOI: 10.1002/ijc.33406] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
7 Wang Z, Han Q, Wang J, Yao W, Wang L, Li K. Rapamycin induces autophagy and apoptosis in Kaposiform hemangioendothelioma primary cells in vitro. Journal of Pediatric Surgery 2022. [DOI: 10.1016/j.jpedsurg.2022.02.032] [Reference Citation Analysis]
8 Lim YH, Fraile C, Antaya RJ, Choate KA. Tufted angioma with associated Kasabach-Merritt phenomenon caused by somatic mutation in GNA14. Pediatr Dermatol 2019;36:963-4. [PMID: 31423605 DOI: 10.1111/pde.13979] [Reference Citation Analysis]
9 Yao W, Li KL, Qin ZP, Li K, Zheng JW, Fan XD, Ma L, Zhou DK, Liu XJ, Wei L, Li L, Tai MZ, Wang JH, Ji Y, Zhou L, Huang HJ, Gao XY, Huang ZJ, Gu S, Yang HY. Standards of care for Kasabach-Merritt phenomenon in China. World J Pediatr 2021;17:123-30. [PMID: 32851561 DOI: 10.1007/s12519-020-00379-9] [Reference Citation Analysis]
10 Wang Y, Wang S, Wang L, Bi S, Zhang J, Zha P, Dai L. Transarterial Embolization in Neonatal Kasabach-Merritt Syndrome. Front Pediatr 2021;9:788120. [PMID: 34926356 DOI: 10.3389/fped.2021.788120] [Reference Citation Analysis]
11 Cabrera TB, Speer AL, Greives MR, Goff DA, Menon NM, Reynolds EW. Sirolimus for Kaposiform Hemangioendothelioma and Kasabach-Merritt Phenomenon in a Neonate. AJP Rep. 2020;10:e390-e394. [PMID: 33214934 DOI: 10.1055/s-0040-1718901] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
12 Chundriger Q, Tariq MU, Abdul-Ghafar J, Ahmed A, Din NU. Kaposiform Hemangioendothelioma: clinicopathological characteristics of 8 cases of a rare vascular tumor and review of literature. Diagn Pathol 2021;16:23. [PMID: 33722245 DOI: 10.1186/s13000-021-01080-9] [Reference Citation Analysis]
13 Kim J, Kim YH, Kim H, Chang BS, Lee CK, Chang SY. Kaposiform Hemangioendothelioma in Adolescent-Onset Scoliosis: A Case Report and Review of Literature. Case Rep Orthop 2020;2020:1839053. [PMID: 32089925 DOI: 10.1155/2020/1839053] [Reference Citation Analysis]
14 Shan Y, Tian R, Gao H, Zhang L, Li J, Xie C, Liang Y, Chen Y, Wang J, Xu M, Gu S. Sirolimus for the treatment of kaposiform hemangioendothelioma: In a trough level-dependent way. J Dermatol 2021;48:1201-9. [PMID: 33932303 DOI: 10.1111/1346-8138.15905] [Reference Citation Analysis]
15 Belmesk L, Dubois J, Caouette-Laberge L, David M, Bortoluzzi P, Kokta V, Hatami A, McCuaig CC. Kaposiform hemangioendothelioma with overlapping features of rapidly involuting congenital hemangioma and a delayed complication of necrotizing fasciitis. Pediatr Dermatol 2020;37:902-6. [PMID: 32677125 DOI: 10.1111/pde.14262] [Reference Citation Analysis]
16 Đuričić S, Sarajlija A, Đokić D, Simić R. Very rare mediastinal location of Kaposiform haemangioendothelioma: A case report and a brief review of the previously published cases. Scripta Medica 2020;51:61-6. [DOI: 10.5937/scriptamed51-25350] [Reference Citation Analysis]
17 Der Sarkissian SA, Wong XL, Kossard S, Hong A, Sebaratnam DF. Kaposiform haemangioendothelioma in an adult: lack of response to topical sirolimus and response to radiotherapy. Clin Exp Dermatol 2022;47:192-3. [PMID: 34480811 DOI: 10.1111/ced.14928] [Reference Citation Analysis]
18 Morais TML, Sánchez-Romero C, Ribeiro L, Faé DS, Verner FS, de Almeida OP, de Aquino SN. Kaposiform Hemangioendothelioma of the Oral Cavity: A Rare Tumor with an Unusual Location. Head Neck Pathol 2021. [PMID: 33715098 DOI: 10.1007/s12105-021-01316-6] [Reference Citation Analysis]